Variant #0000849831 (NC_000002.11:g.25013423del, NM_004036.3:c.*29378del (ADCY3))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.25013423del
DNA change (hg38) -
Published as -
ISCN -
DB-ID ADCY3_000015
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PTRHD1 NM_001013663.1 +?/. - c.280del r.(?) p.(Leu94Trpfs*40)
ADCY3 NM_004036.3 +?/. - c.*29378del r.(?) p.(=)
CENPO NM_024322.2 +?/. - c.-3035del r.(?) p.(=)


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